{
    "disease_id": "DOID:0111378",
    "recommended_name": {
        "id": "DOID:0111378",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111378",
        "name": "fetal akinesia deformation sequence syndrome 2",
        "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in RAPSN on chromosome 11p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111378",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111378",
            "name": "FADS2",
            "description": ""
        },
        {
            "id": "MIM:618388",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618388",
            "name": "Fetal akinesia deformation sequence 2",
            "description": "Fetal akinesia deformation sequence 2"
        }
    ]
}